Yang Qiu-Jin, Zheng Jie, Dang Fu-Tao, Wan Yue-Meng, Yang Jing
Department of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
Medicine (Baltimore). 2020 Aug 28;99(35):e21848. doi: 10.1097/MD.0000000000021848.
Drug-induced pancreatitis (DIP) is a kind of acute pancreatitis with a relatively low incidence. There are many cases of acute pancreatitis (AP) caused by chemotherapeutic agents that have been reported. However, few reports focus on the combination of chemotherapeutic agents that induce acute pancreatitis. This article aims to retrospectively analyze a case of DIP and to explore the relationship between chemotherapeutic agents and acute pancreatitis.
Here, we report a 35-year-old Chinese female patient who was diagnosed as acute myeloid leukemia with BCR/ABL expression. After induction chemotherapy of daunorubicin and cytarabine, bone marrow aspiration showed: Acute myeloid leukemia-not relieved (AML-NR). Then the regimen of homoharringtonine, cytarabine and dasatinib was started. The patient developed abdominal pain on the 14th day of chemotherapy. Laboratory tests showed elevated serum amylase (AMY) and lipase (LIPA). Computed tomography (CT) of the abdomen revealed a swollen pancreas with blurred edges and thickened left prerenal fascia.
The patient was diagnosed as DIP by the symptoms of upper abdominal pain and the change of CT images. Other common causes of AP were excluded meanwhile.
The chemotherapy was stopped immediately. And after fasting, fluid infusion and inhibiting the secretion of the pancreas, the symptoms were relieved.
DIP relapsed when the regimen of aclacinomycin + cytarabine + G-CSF + dasatinib regimen (G-CSF (400ug/day, day 1 to 15), cytarabine (30 mg/day, day 2 to 15), aclacinomycin (20 mg/day, day 2 to 5)and dasatinib (140 mg/day, continuously)) was given, and was recovered after treatment for AP was performed.
To choose the best treatment plan for patients, clinicians should raise awareness of DIP, and should know that chemotherapeutic agents can induce pancreatitis and the combination of chemotherapeutic agents may increase the risk of drug-induced pancreatitis.
药物性胰腺炎(DIP)是一种发病率相对较低的急性胰腺炎。已有许多关于化疗药物引起急性胰腺炎(AP)的病例报道。然而,很少有报道关注诱发急性胰腺炎的化疗药物组合。本文旨在回顾性分析1例DIP病例,并探讨化疗药物与急性胰腺炎之间的关系。
在此,我们报告1例35岁中国女性患者,诊断为伴有BCR/ABL表达的急性髓系白血病。在接受柔红霉素和阿糖胞苷诱导化疗后,骨髓穿刺显示:急性髓系白血病未缓解(AML-NR)。随后开始高三尖杉酯碱、阿糖胞苷和达沙替尼方案。患者在化疗第14天出现腹痛。实验室检查显示血清淀粉酶(AMY)和脂肪酶(LIPA)升高。腹部计算机断层扫描(CT)显示胰腺肿大,边缘模糊,左肾前筋膜增厚。
根据上腹部疼痛症状及CT图像变化,该患者被诊断为DIP。同时排除了AP的其他常见病因。
立即停止化疗。禁食、补液并抑制胰腺分泌后,症状缓解。
在给予阿克拉霉素+阿糖胞苷+粒细胞集落刺激因子(G-CSF)+达沙替尼方案(G-CSF(400μg/天,第1至15天),阿糖胞苷(30mg/天,第2至15天),阿克拉霉素(20mg/天,第2至5天),达沙替尼(140mg/天,持续使用))时,DIP复发,在进行AP治疗后恢复。
为患者选择最佳治疗方案时,临床医生应提高对DIP的认识,应知晓化疗药物可诱发胰腺炎,且化疗药物组合可能增加药物性胰腺炎的风险。